| アブストラクト | BACKGROUND: The comprehensive quantitative and comparative risk data of drug-induced erectile dysfunction (ED) are still lacking, and this study aims to supplement this information. RESEARCH DESIGN AND METHODS: We reviewed all the ED reports in the FDA Adverse Event Reporting System (FAERS) database from 2004 to 2023 and summarized a potential ED culprit-drug list and its corresponding reporting frequency. The reporting odds ratio (ROR) method was used to conduct disproportionality analysis. RESULTS: A total of 20,098 ED reports were retrieved from the FAERS database, which recorded 734 different ED culprit-drugs, involving 74 drug classes. Finasteride was the drug with the highest reporting frequency, and urologicals was the drug class with the highest reporting frequency. In disproportionality analysis, 209 drugs with positive signals showed a close relationship with ED occurrence, among which finasteride was the drug with the highest signal strength. Among 209 drugs with positive signals, 27 were compound preparations, and the risk level of compound preparations was usually higher than their single active ingredient. CONCLUSIONS: Our study integrated quantitative and comparative ED risk data of 734 drugs by using the FAERS database, which can provide reference information for regulators, medical personnel, and others involved in drug management and use. |
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| ジャーナル名 | Expert opinion on drug safety |
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| Pubmed追加日 | 2024/8/23 |
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| 投稿者 | Li, Dongxuan; Dai, Liyang; Zhu, Jun; Wang, Yalan; Zhang, Rui; Wu, Fan; Zhang, Tongyan; Liu, Songqing; Du, Qian |
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| 組織名 | Department of Pharmacy, The Third Affiliated Hospital of Chongqing Medical;University, Chongqing, China.;Center for Medical Information and Statistics, The Third Affiliated Hospital of;Chongqing Medical University, Chongqing, China.;College of Pharmacy, Chongqing Medical University, Chongqing, China.;Infectious Disease Department, Second Affiliated Hospital of Tianjin University;of Traditional Chinese Medicine, Tianjin, China. |
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| Pubmed リンク | https://www.ncbi.nlm.nih.gov/pubmed/39175438/ |
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